CDMO Services
Your trusted partner for pharmaceutical development & manufacturing
At Galenica, we provide comprehensive pharmaceutical development and manufacturing solutions, offering expertise in formulation and process development, analytical services, and GMP-compliant manufacturing. With over 25 years of experience, we have supported 100+ clients, bringing some of their pharmaceutical innovations to market. Our facilities and expert teams ensure seamless execution from preclinical development to full-scale production.
Whether you need assistance with early-stage formulation, clinical trial material (CTM) production, or large-scale manufacturing, Galenica is your reliable and flexible CDMO partner. By choosing Galenica, you gain access to a team dedicated to solving complex formulation challenges while maintaining regulatory compliance and delivering high-quality results on time.
Why choose Galenica?
- Over 25 years of experience in pharmaceutical development.
- GMP-compliant operations ensuring high-quality standards.
- Vast experience in regulatory support.
- Flexible and scalable manufacturing solutions.
- Strong expertise in formulation development for various dosage forms.
- Customized solutions tailored to client needs.
Our CDMO Services – Tailored pharmaceutical development
At Galenica, we provide comprehensive contract development and manufacturing (CDMO) services, supporting pharmaceutical companies from early-stage formulation to clinical trial materials and commercial-scale production. With expertise in small molecules and peptides, we offer customized solutions to meet diverse development needs.
Our core services include:
Pharmaceutical Development: Tailor-made formulations for oral, dermal, nasal, and pulmonary dosage forms, ensuring optimal bioavailability and stability.
Analytical & Stability Testing: Advanced method development, validation, and QC testing to guarantee compliance with industry regulations.
GMP Manufacturing & Scale-Up: Flexible batch production for solids, liquids, and semi-solids, including high-potency compound handling.
Regulatory & CMC Support: Guidance through IND, IMPD, NDA, and ANDA applications to facilitate a seamless approval process.
Our state-of-the-art facilities, cutting-edge technology, and experienced team ensure precision, compliance, and efficiency at every stage of drug development.
Key features of our pharmaceutical services
End-to-End Support: From preclinical research to manufacturing and release for Phase I-III clinical trials and full-scale production, ensuring a smooth development process.
Versatile Manufacturing: Expertise in solids, semi-solids, and liquids, utilizing state-of-the art process technologies.
Advanced Analytical Capabilities: Experienced team for complex Analytical Development and comprehensive quality control, stability testing, and regulatory support.
Specialized Handling: Safe processing of high-potency compounds and moisture-sensitive formulations.
Innovation & Optimization: Expertise in multiparticulates and DoE-based formulation design.
Uncompromising Quality: We adhere to GMP and ICH guidelines, audited by the Swedish Medical Products Agency (Läkemedelsverket), ensuring the highest industry standards.
Galenica’s flexible, solution-oriented approach ensures that your pharmaceutical development process is efficient, cost-effective, and aligned with regulatory expectations. Whether you require tailor-made formulation development, analytical support, or small scale production, we are here to guide and support you every step of the way.
Looking for a trusted CDMO partner? Discover how Galenica can accelerate your pharmaceutical development. Contact us!